Emphasized topics
-Clinical trials
planning, acquiring administrative and ethical permissions, coordination, site management, monitoring. Recruitment management. Directing international clinical groups.
- Preparing feasibility studies for the trials
- Completing the start-up procedure
- Pre-study Site Evaluation and Investigator Assessments
- Site Initiation
- Site Training
- Monitoring Activities Associated with Phase II-IV Clinical Research Trials (Interim Monitoring)
- Comprehensive Trip Reports
- Drug...
